Anti-inflammatory Effects of Aspalathin and Nothofagin from Rooibos (Aspalathus linearis) In Vitro and In Vivo

被引:43
|
作者
Lee, Wonhwa [1 ,2 ]
Bae, Jong-Sup [1 ]
机构
[1] Kyungpook Natl Univ, Pharmaceut Sci Res Inst, CMRI, Coll Pharm, Taegu 702701, South Korea
[2] Kyungpook Natl Univ, Sch Med, Dept Biochem & Cell Biol, Plus KNU Biomed Convergence Program BK21, Taegu 702701, South Korea
基金
新加坡国家研究基金会;
关键词
aspalathin; nothofagin; lipopolysaccharide; endothelium; inflammation; barrier integrity; NF-KAPPA-B; ADHESION MOLECULE EXPRESSION; ENDOTHELIAL-CELL MONOLAYERS; NITRIC-OXIDE SYNTHASE; ACTIVATED PROTEIN-KINASE; LOW-DENSITY-LIPOPROTEIN; AFRICAN HERBAL TEAS; GROUP BOX 1; TNF-ALPHA; BARRIER DYSFUNCTION;
D O I
10.1007/s10753-015-0125-1
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Aspalathin (Asp) and nothofagin (Not) are two major active dihydrochalcones found in green rooibos, which have been reported for their anti-oxidant activity. Here, we investigated the anti-inflammatory effects and underlying mechanisms of Asp and Not against lipopolysaccharide (LPS)-mediated vascular inflammatory responses. The anti-inflammatory activities of Asp and Not were determined by measuring permeability, monocytes adhesion and migration, and activation of pro-inflammatory proteins in LPS-activated human umbilical vein endothelial cells (HUVECs) and mice. We found that each compound inhibited LPS-induced barrier disruption, expression of cell adhesion molecules (CAMs), and adhesion/transendothelial migration of neutrophils to human endothelial cells. Asp and Not also suppressed LPS-induced hyperpermeability and leukocyte migration in vivo. Furthermore, each compound suppressed the production of tumor necrosis factor-alpha (TNF-alpha) or interleukin (IL)-6 and the activation of nuclear factor-kappa B (NF-kappa B) or extracellular regulated kinases (ERK) 1/2 by LPS. Moreover, treatment with each compound resulted in reduced LPS-induced lethal endotoxemia. These results suggest that Asp and Not posses anti-inflammatory functions by inhibiting hyperpermeability, expression of CAMs, and adhesion and migration of leukocytes, thereby endorsing its usefulness as a therapy for vascular inflammatory diseases.
引用
收藏
页码:1502 / 1516
页数:15
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